Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
  • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
  • A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
  • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
  • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
  • A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
  • A01N47/14—Di-thio analogues thereof
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
  • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
  • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
  • A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P33/00—Antiparasitic agents
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
  • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Definitions

• the present invention relates to a novel oxadiazoline derivative and agrochemical composition comprising it.
• a large number of synthetic compounds having pest-controlling activities have so far been used as insecticides. Most of them, however, belong to the family of organic phosphoric acid esters, carbamic acid esters, organic chlorine-containing compounds or pyrethroid compounds .
• 1-arylpyrazole derivatives having a hydrogen or halogen atom or an alkyl, cycloalkyl, haloalkyl, cyano, nitro, carbamoyl or thiocarbamoyl group at position 3 of the pyrazole ring exhibit insecticidal activity [ JP-A-228065/1987 , 207259/1987, 148240/1993, 282366/1990, 86054/1993, and JP-A-500319/1995, etc.].
• the present inventors have long been engaged in intensive investigations in an attempt to discover insecticides quite different in structure from the insecticides that have so far been used. As a result, they unexpectedly found that novel oxadiazolinylpyrazole derivatives represented by the formula [I], inclusive of salts thereof, have very strong insecticidal activity. It was further found that they have little phytotoxicity, are low in toxicity and safe to humans and animals, to fish and to natural enemies to pests, among others. Based on these findings, the present inventors have continued their research, and have now completed the present invention.
• the present invention relates to: [ 1 ] a compound represented by the formula [ I ] :
• R 1 is a C 1 . 6 alkyl group or a C x _ 6 haloalkyl group; n is 0, 1 or 2; X is (1) a group of -NR 2 R 3 wherein R 2 and R 3 independently represent (i) a hydrogen atom or (ii) a C x _ 6 alkyl group which may optionally be substituted with pyridyl group,
• R 5 is an optionally substituted alkyl group or an optionally substituted acyl group
• R 8 is (1) a halogen atom, (2) a C x _ 6 haloalkyl group, (3) a
• A is ( 1 ) a nitrogen atom or ( 2 ) a group of ⁇ .
• R 9 is a chlorine atom or cyano; and B is a nitrogen atom or
• 10 alkanoyl group which may optionally be substituted with one to three substituents selected from the group consisting of (i) amino which may optionally be substituted with one or two C x _ 6 alkyl groups, (ii) a C___ 6 alkoxy group, (iii) phenyl and (iv) a halogen atom, (3) a C 4 . 10 cycloalkanoyl group, (4) a C 3 .
• alkenylcarbonyl group (5) benzoyl, (6) carbamoyl which may optionally be substituted with one or two substituents selected from the group consisting of (i) a C x , 6 alkyl group which may optionally be substituted with the substituents selected from the group consisting of phenyl, halogen and amino which may optionally be substituted with C x _ 6 alkyl, (ii) a C 3 . 9 cycloalkyl group, (iii) a C 2 . 6 alkenyl group, (iv) a C 2 .
• R 8 is trifluoromethyl
• B is a nitrogen atom, or a salt thereof
• an agrochemical composition which comprises an effective amount of the compound as described in above [ 1 ] or a salt thereof, [ 17 ] the agrochemical composition as described in above [ 16 ] , which is an insecticidal composition,
• [18] a method of combatting an insect, which comprises applying or administering an effective dose of the compound as described in above [1] or a salt thereof to a vertebrate, a paddy field, plowland, orchard, non-cropland or house,
• the compound of the above formula [ I ] or a salt thereof of the present invention sometimes have geometrical isomers and/or stereoisomers, and the present invention includes all of these isomers or mixtures of them.
• the C x _ 6 alkyl group for R 1 includes methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, or tert-butyl .
• the C___ 6 haloalkyl group for R 1 includes a alkyl group which is substituted with one to ten (preferably one to five) halogen atoms (e.g. fluorine, chlorine, bromine, iodine) such as chloromethyl, fluoromethyl, bromomethyl,
• halogen atoms e.g. fluorine, chlorine, bromine, iodine
• n 0, 1 or 2, and preferred is 1.
• R 1 is especially preferably C x _ 6 haloalkyl group such as trifluoromethyl.
• C 1 _ 6 alkyl group in "C__ 6 alkyl group which may optionally be substituted with pyridyl group” includes the same ones as mentioned in the above C ⁇ _ 6 alkyl group for
• the pyridyl group in the definition of R 2 and R 3 includes 2-, 3- or 4-pyridyl.
• the alkyl group may be substituted with one or two pyridyl groups.
• R 2 and R 3 preferably represent a hydrogen atom or methyl. Particularly, both R 2 and R 3 are preferably a hydrogen atom.
• the C x _ 6 alkyl group for R , R 6 and R 7 includes the same ones as mentioned in the above alkyl group for R 1 .
• R 4 is preferably a C x _ 6 alkyl group. Especially preferred is ethyl or isopropyl.
• R 6 and R 7 are preferably a C___ 6 alkyl group such as methyl.
• the C x _ 3 alkoxy group which may be on the phenyl group for Ar includes methoxy, ethoxy, propoxy or isopropoxy. Especially preferred is methoxy.
• the phenyl group for Ar may optionally be substituted with one to three substituents selected from the group consisting of hydroxy and the C x _ 3 alkoxy group.
• Ar is preferably 3-methoxy- 4-hydroxyphenyl group.
• the pyrrolyl group for X includes 1- , 2- or 3-pyrrolyl group.
• the alkyl group in "an optionally substituted alkyl group” for R 5 includes the same ones as mentioned in the alkyl group for R 1 .
• the substituent of the alkyl group includes hydroxy, amino, a mono- or alkylamino group (e.g. methylamino, ethylamino, propylamino, dimethylamino, diethylamino, etc.), a C x . 6 alkoxy group (e.g. methoxy, ethoxy, propoxy, isopropoxy, butoxy, etc. ) , a C x _ 4 alkylthio group (e.g.
• a C ⁇ alkoxy group is particularly preferable.
• the number of the substituents is one to six, preferably one to three, within the substitutable range.
• a C-__ 20 acyl group derived from carboxylic acid is used. Specifically, for example, (1) formyl, (2) an alkanoyl group, preferably a C 2 .
• alkanoyl group e.g. C x _ 9 alkyl-carbonyl such as acetyl, propionyl, butylyl, isobutylyl, pentanoyl, hexanoyl, heptanoyl, pivaloyl, etc.
• a cycloalkanoyl group preferably a C 4 .
• cycloalkanoyl group e.g. cyclopropylcarbonyl , cyclobutylcarbonyl, cyclopentylcarbonyl , cyclohexylcarbonyl, etc.
• an alkenylcarbonyl group preferably a C 3 .
• alkenylcarbonyl group e.g. acryloyl, allylcarbonyl, isopropenylcarbonyl, isobutenylcarbonyl, 1-methylallylcarbonyl, cinnamoyl, etc.
• an alkynylcarbonyl group preferably a C 3 . 7 alkynylcarbonyl group (e.g. propargylcarbonyl , 2- butynylcarbonyl , 3-butynylcarbonyl , 3-pentynylcarbonyl, etc.)
• an arylcarbonyl group preferably a C 6 . 14 aryl- carbonyl group (e.g.
• an alkoxycarbonyl group preferably a C ⁇ alkoxy-carbonyl group (e.g. methoxycarbonyl, ethoxycarbonyl , propoxycarbonyl , isopropoxycarbonyl, butoxycarbonyl, isobutoxycarbonyl, sec-butoxycarbonyl, tert-butoxycarbonyl, etc.), (8) an aryloxycarbonyl group, preferably a C 6 . 14 aryloxy-carbonyl group (e.g.
• phenoxycarbonyl , ( 9 ) an aralkylcarbonyl group, preferably a C 7 _ 19 aralkyl-carbonyl group (e.g. phenyl-C- ⁇ alkylcarbonyl such as benzylcarbonyl, phenethylcarbonyl or phenylpropylcarbonyl; benzhydrylcarbonyl; naphthyl-Ci. 4 alkylcarbonyl such as 1-naphthylethylcarbonyl, etc.), (10) an aralkyloxycarbonyl group, preferably a C 7 . 19 aralkyloxycarbonyl group (e.g.
• phenyl-C ⁇ alkyloxycarbonyl such as benzyloxycarbonyl, phenethyloxycarbonyl, phenylpropyloxycarbonyl, etc.
• (11) carbamoyl or (12) a cyclic aminocarbonyl group e.g. 1-pyrrolidinocarbonyl, piperidinocarbonyl, morpholinocarbonyl, thiomorpholinocarbonyl , 1-perhydroazepinylcarbonyl, etc.
• each group may optionally have one to six (preferably one to three) substituents selected from the group consisting of hydroxy, amino, a mono- or alkylamino group (e.g. methylamino, ethylamino, propylamino, dimethylamino, diethylamino, etc.), a C x _ 6 alkoxy group (e.g. methoxy, ethoxy, propoxy, isopropoxy. butoxy, etc.), a C 1-6 alkylthio group (e.g.
• acyl group is cycloalkanoyl, arylcarbonyl , alkoxycarbonyl, aryloxycarbonyl, aralkylcarbonyl or aralkyloxycarbonyl, each group may optionally have one to five (preferably one to three) substituents selected from the group consisting of hydroxy, amino, a mono- or alkylamino group (e.g.
• a C x _ 6 alkoxy group e.g. methoxy, ethoxy, propoxy, isopropoxy, butoxy, etc.
• a C 1 _ 6 alkylthio group e.g. methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, etc.
• halogen e.g.
• a C x _ 6 alkyl group e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, etc.
• a C 2 . 6 alkenyl group e.g. vinyl, allyl, 1-propenyl, 1-butenyl, 2-butenyl, etc.
• a C 2tician 6 alkynyl group e.g. ethynyl, 1-propynyl, propargyl, 1-butynyl, etc.
• the carbamoyl may optionally have one or two substituents selected from the group consisting of (1) a C x _ 6 alkyl group (e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, etc.), (2) a C 3 . 9 cycloalkyl group (e.g. cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc.), (3) a C 2 . 6 alkenyl group (e.g.
• a C x _ 6 alkyl group e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, etc.
• a C 3 . 9 cycloalkyl group e.g.
• substituents may form a cyclic amino group (e.g. 1-pyrrolidino, piperidino, morpholino, thiomorpholino, 4-methyl-l-piperadino, etc.) together with an adjacent nitrogen atom.
• substituents may further optionally be substituted with one to six (preferably one to three) substituents selected from the group consisting of hydroxy, amino, a mono- or di-C ⁇ alkylamino group (e.g.
• a C x _ 6 alkoxy group e.g. methoxy, ethoxy, propoxy, isopropoxy, butoxy, etc.
• a C___ 6 alkylthio group e.g. methylthio, ethylthio, n-propylthio, isopropylthio, n-butylthio, etc.
• halogen e.g. fluorine, chlorine, bromine, iodine
• phenyl, carboxyl, nitro and cyano e.g. fluorine, chlorine, bromine, iodine
• R 5 is preferably an optionally substituted alkyl group, an optionally substituted alkanoyl group, an optionally substituted cycloalkanoyl group, an optionally substituted alkenylcarbonyl group, an optionally substituted arylcarbonyl group, an optionally substituted alkoxycarbonyl group or an optionally substituted carbamoyl group, and is more preferably an optionally substituted carbamoyl group.
• particularly preferred is (1) a C x _ 6 alkyl group which may optionally be substituted with one to three C x _ 6 alkoxy groups , ( 2 ) a C 2 .
• alkenylcarbonyl group (5) benzoyl, (6) carbamoyl which may optionally be substituted with one or two substituents selected from the group consisting of (i) a C x _ 6 alkyl group which may optionally be substituted with one to three substituents selected from the group consisting of phenyl, halogen and amino which may optionally be substituted with one or two C x _ 6 alkyl groups, (ii) a C 3 . 9 cycloalkyl group, (iii) a C 2 . 6 alkenyl group, (iv) a C 2 .
• the halogen for R 8 includes fluorine, chlorine, bromine or iodine.
• the C x _ 6 haloalkyl group for R 8 includes the same ones as mentioned in the C ⁇ haloalkyl group for R 1 .
• the C x _ 6 haloalkoxy group for R 8 includes a C x _ 6 alkoxy group which is substituted with one to ten (preferably one to five) halogen atoms (e.g. fluorine, chlorine, bromine, iodine) such as chloromethoxy, fluoromethoxy, bromomethoxy, 2-chloroethoxy, dichloroethoxy, trichloromethoxy, trifluoromethoxy, 2,2,2- trifluoroethoxy , pentafluoroethoxy, heptafluoropropoxy or nonafluorobutoxy. Particularly preferred is trifluoromethoxy .
• the C ⁇ _ 6 haloalkyl group in the "phenyl which may optionally be substituted with a C _ 6 haloalkyl group” includes the same ones as mentioned in the C x _ 6 haloalkyl group for R 1 .
• the number of the substituents on the phenyl is one to five, preferably one to three. Particularly, phenyl which may optionally be substituted with one to three trifluoromethyl groups is preferable.
• A is preferably
• B is preferably a nitrogen atom.
• n is 0 , 1 or 2 ;
• R 5 is (1) a C- L . 6 alkyl group which may optionally be substituted with a C ⁇ alkoxy group, (2) a C x . 9 alkylcarbonyl group which may optionally be substituted with one to three substituents selected from the group consisting of a mono- or di-C ⁇ alkylamino group, phenyl, a C x _ 6 alkoxy group and halogen, (3) benzoyl, (4) a C 4 . 10 cycloalkanoyl group, (5) a C 3 . 10 alkenylcarbonyl group which may optionally be substituted with one or two phenyl, (6) formyl, (7) a C 1 .
• carbamoyl which may optionally be substituted with one or two substituents selected from the group consisting of a C x _ 6 alkyl group, a C 2 . 6 alkenyl group, a C 2 . 6 alkynyl group, phenyl, benzyl, a mono- or alkylamino, hydroxy, a C x _ 6 alkoxy group, a C 3 .
• More preferable compound [ I ] is a compound represented by the formula:
• n is 0 , 1 or 2 ;
• R b is (1) a Cj.g alkyl-carbonyl group or (2) carbamoyl which may optionally be substituted with one or two C x _ 6 alkyl groups .
• n is 0 , 1 or 2 ;
• the salt of the compound [ I ] of the present invention may be any agrochemically acceptable salt . That is , when the compound [ I ] has an acidic group such as a carboxyl group, a sulfo group, etc. in the molecule, the compound [I] may form a salt with a base.
• the base for example, there can be used inorganic bases such as alkali metal, e.g. sodium, potassium, lithium; alkaline earth metal, e.g.
• the compound [I] may form a salt with an acid.
• the acid for example, there can be used salts of inorganic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid, sulfuric acid, perchloric acid and the like; and salts of organic acids such as formic acid, acetic acid, tartaric acid, malic acid, citric acid, oxalic acid, succinic acid, benzole acid, picric acid, methanesulfonic acid, p-toluenesulfonic acid and the like.
• the compound [ I ] may form an intramolecular salt and the case is also included in the present invention.
• the compound [I] or a salt thereof of the present invention and the compound [II] shown below which serve as starting materials in the production of the compound [I] or a salt thereof can be produced by the process described in WO 97/28126 or analogous processes thereof.
• the compound [I] or a salt thereof according to the present invention can be synthesized by reacting the starting compound [ II ] with an acylating agent or an alkylating agent, optionally in the presence of an appropriate acid or base catalyst.
• the acylating agent to be used in such reaction includes known acylating agents such as carboxylic acid halides (e.g. acetyl chloride, propionyl bromide, etc.), carbamoyl halides (e.g. N,N- dimethylcarbamoyl chloride, N,N-diethylcarbamoyl chloride, etc.), halocarbonic acid esters (e.g.
• the alkylating agent to be used in such reaction includes known alkylating agents such as alkyl halides (e.g. methyl iodide , ethyl bromide, etc.), alkyl sulfonates (e.g.
• acylating agent or alkylating agent mentioned above is not particularly restricted. Said agent may be used in large excess so that it may serve as a solvent as well.
• the base catalyst to be used in this reaction includes alkali metal alcoholates such as sodium ethylate, sodium methylate and potassium tert-butoxide; organic bases such as triethylamine, diisopropylethylamine, pyridine, 4- dimethylaminopyridine and N,N-dimethylaniline; and inorganic bases such as potassium carbonate, sodium carbonate, sodium hydroxide, potassium hydroxide, sodium hydrogen carbonate, potassium hydrogen carbonate and sodium hydride.
• the amount of the base to be used is not particularly restricted provided that it does not adversely affect the reaction.
• the base may be used in large excess so that it may serve as a solvent as well .
• a preferred amount is 0.1 to 20 equivalents, however.
• the acid catalyst to be used in this reaction includes inorganic protic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid and sulfuric acid; organic protic acids such as formic acid, acetic acid, tartaric acid, malic acid, citric acid, oxalic acid, succinic acid, benzoic acid, trifluoroacetic acid and p-toluenesulfonic acid; and Lewis acids such as aluminum chloride, ferric chloride, zinc chloride. titanium tetrachloride and boron trifluoride.
• the amount of the acid catalyst to be submitted to the reaction is not particularly restricted unless it adversely affects the reaction.
• the acid catalyst may be used in large excess so that it may serve as a solvent as well. Preferably, it is used in an amount of 0.1 to 20 equivalents.
• This reaction can be carried out using an appropriate solvent.
• solvent is not restricted to any particular species provided that it does not react with the substrate, reagent or product of the reaction. Those solvents which can dissolve both the reaction substrate and reaction reagent are preferred, however.
• solvents there may be mentioned, for example, aliphatic hydrocarbons such as pentane, hexane, heptane and petroleum ether; aromatic hydrocarbons such as benzene, toluene and xylene; esters such as methyl acetate, ethyl acetate, ethyl formate and ethyl propionate; ketones such as acetone and methyl ethyl ketone; ethers such as diethyl ether, dipropyl ether, diisopropyl ether, dibutyl ether, tetrahydrofuran and dioxane; nitriles such as acetonitrile and propionitrile; acid amides such
• the compounds [I] When the compounds [I] are obtained in the free form, they may be converted to a form of salts such as mentioned above and, when they are obtained in the form of salts, they may respectively be converted to the free form in the conventional manner.
• the starting compound In cases where a compound included in the group of compounds [I] is used as a starting material for the production of another compound of formula [I] , the starting compound may be used either in the free form or in the form of a salt. If other raw materials can take the form of salts such as mentioned above, they also may be used either in the free form or in the form of such salts. Therefore, it is to be noted that the raw materials and products mentioned in the description of the production processes given below include also salts thereof (e.g. salts with acids such as mentioned with reference to the compounds [ I ] ) .
• R S represents an optionally substituted C ⁇ ,, alkyl group, an optionally substituted C 3 . 9 cycloalkyl group, an optionally substituted C 2 . 6 alkenyl group, an optionally substituted phenyl group, a C x _ 6 alkoxy group, or a mono- or alkylamino group
• R 5b represents an optionally substituted C ⁇ ,, alkyl group, an optionally substituted C 3 . 9 cycloalkyl group, an optionally substituted C 2 .
• R 5 ⁇ , R 5£ and R 53 independently represent an optionally substituted C _ 6 alkyl group; m is 1 or 2; R 5d and R 5e independently represent a hydrogen atom, an optionally substituted C x _ 6 alkyl group, an optionally substituted C 3 . 9 cycloalkyl group, an optionally substituted C 2 . 6 alkenyl group, an optionally substituted C 2 . 6 alkynyl group, an optionally substituted phenyl group, a mono- or di-C ⁇ alkylamino group, a cyclic amino group, hydroxy, a C ⁇ alkoxy group. or R 5d and R 5e may be combined to form a cyclic amino group together with an adjacent nitrogen atom.
• the alkyl group in the optionally substituted C ⁇ ,, alkyl group for R 5a and R s includes methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, neo-pentyl, 1-ethylpropyl, 1-propylbutyl, n- hexyl, n-heptyl, n-octyl, or n-nonyl, etc.
• the substituent for the alkyl group includes the same ones as mentioned for the substituent of the optionally substituted alkyl group of R 5 .
• the number of the substituents is one to six, preferably one to three, within the substitutable range.
• the optionally substituted C 1-6 alkyl group for R Sc , R 5d , R 5e , R 5f and R 59 includes the same ones as mentioned for the optionally substituted alkyl group of above-mentioned R 5 .
• the substituent for the phenyl group of R 5a , R 5b , R 5d and R 5e includes the same ones as mentioned for the substituent on the acyl group (arylcarbonyl group) of above-mentioned R 5 .
• the number of the substituents is one to five, preferably one to three.
• the C x . 6 alkoxy group for R 5a , R 5d and R 5e includes methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, sec-butoxy, or tert-butoxy, etc.
• the C x _ 6 alkyl group in the mono- or di-C ⁇ alkylamino group for R 5a , R 5d and R 5e includes the same ones as mentioned for the alkyl group of above-mentioned R 1 .
• the cycloalkyl group in the optionally substituted 3 . 9 cycloalkyl group includes cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, etc.
• the alkenyl group in the optionally substituted C 2 . 6 alkenyl group for R 5a , R 5b , R 5d and R 5e includes vinyl, allyl, 1-propenyl, 1-butenyl, or 2-butenyl, etc.
• the alkynyl group in the optionally substituted C 2 . 6 alkynyl group for R 5d and R 5e includes ethynyl, 1-propynyl, propargyl, or 1-butynyl, etc.
• the cyclic amino group for R 5d and R 5e includes 1- pyrrolidino, piperidino, morpholino, or 4-methyl-l- piperazino, etc.
• cycloalkyl, alkenyl, alkynyl or cyclic amino group may optionally be substituted with one to six (preferably one to three) substituents selected from the group consisting of hydroxy, amino, a mono- or di- C x _ 6 alkylamino group (e.g. methylamino, ethylamino, propylamino, dimethylamino, diethylamino, etc.), a C x _ 6 alkoxy group (e.g. methoxy, ethoxy, propoxy, isopropoxy, butoxy, etc.), a C 1 _ 6 alkylthio group (e.g.
• halogen e.g. fluorine, chlorine, bromine, iodine
• phenyl carboxyl, nitro and cyano.
• the cyclic amino group in which R 5d and R 5e may form together with an adjacent nitrogen atom includes 1-pyrrolidino, piperidino, morpholino, or 4-methyl-1- piperazino, etc.
• the reaction schema (A) represents the reaction of a compound [ II ] with an acylating agent of the formula R 5a COL [wherein L represents a leaving group such as a halogen atom (e.g. fluorine, chlorine, bromine, iodine) or an acyloxy group such as a C x . 10 acyloxy group (e.g.
• the compound [II] not only serves as the starting material for this reaction but also has excellent insecticidal activity by itself.
• preferred examples of the compound [II] there may be mentioned l-(2,6- dichloro-4-trifluoromethylphenyl) -5- ethoxymethyleneamino-3- ( ⁇ 2 -l , 2 , 4-oxadiazolin-3-yl) -4- trifluoromethylsulfinylpyrazole, 1- ( 2 , 6-dichloro-4- trifluoromethylphenyl) -3- ( ⁇ 2 -l , 2 , 4-oxadiazolin-3-yl) - 5- (n-propoxymethyleneamino) -4- trifluoromethylthiopyrazole and 1- ( 2 , 6-dichloro-4- trifluoromethylphenyl) -3-( ⁇ 2 -l,2, 4-oxadiazolin-3-yl) - 5- (n-propoxymethyleneamino) -4-
• the amount of the acylating agent mentioned above is not particularly restricted.
• Said agent may be used in large excess so that it may serve as a solvent as well.
• it is used in an amount of about 0.8 to 5 equivalents.
• a base for the purpose of promoting the reaction and reducing the byproduct formation or when the starting material is treated with a base prior to the reaction or the reaction mixture after the reaction is treated with a base
• favorable results can be obtained.
• Usable as such base are, for example, alkali metal alcoholates such as sodium ethylate, sodium methylate and potassium tert-butoxide; organic bases such as triethylamine, diisopropylethylamine, pyridine, 4- dimethylaminopyridine and N,N-dimethylaniline; and inorganic bases such as potassium carbonate, sodium carbonate, sodium hydroxide, potassium hydroxide, sodium hydrogen carbonate, potassium hydrogen carbonate and sodium hydride.
• the amount of the base to be used is not particularly restricted unless it adversely affects the reaction. Said base may be used in large excess so that it may serve as a solvent as well.
• This reaction can be carried out using an appropriate solvent.
• solvent is not restricted to any particular species provided that it does not react with the substrate, reagent or product of the reaction, hence does not cause byproduct formation. Those solvents which can dissolve both the reaction substrate and reaction reagent are preferred, however.
• solvents there may be mentioned, for example, aliphatic hydrocarbons such as pentane, hexane, heptane and petroleum ether; aromatic hydrocarbons such as benzene, toluene and xylene; esters such as methyl acetate, ethyl acetate, ethyl formate and ethyl propionate; ketones such as acetone and methyl ethyl ketone; ethers such as diethyl ether, dipropyl ether, diisopropyl ether, dibutyl ether, tetrahydrofuran and dioxane; nitriles such as acetonitrile and propionitrile; acid amides such as dimethylformamide and dimethylacetamide; sulfoxides such as dimethyl sulfoxide; sulfones such as sulfolane; phosphoric acid amides such as hexamethylphosphoramide;
• the reaction temperature is generally within the range of about -50°C to 200°C, preferably about -30°C to 150°C, and the reaction time is generally within the range of about 0.1 to 96 hours, preferably 0.1 to 72 hours, more preferably about 0.1 to 24 hours.
• the compound obtained can be isolated and purified by per se known means , such as concentration, concentration under reduced pressure, pH adjustment, solvent exchange, solvent extraction, distillation, crystallization, recrystallization, chromatography and the like. Said compound may be submitted to the next reaction either after such isolation/purification or in the form of a reaction mixture .
• the reaction schema (B) represents the reaction of a compound [II] with a carboxylic acid derivative of the formula R 5a C0 2 H [wherein R 5a is as defined above] in the presence of a dehydrative condensing agent to give the corresponding compound [IV].
• the dehydrative condensing agent to be used in this reaction includes known dehydrative condensing agents such as DCC (dicyclohexylcarbodiimide), carbonyldiimidazole, and BOP reagent (benzotriazol-1-yloxy- tris (dimethylamino )phosphonium hexafluorophosphate) .
• the amount to be used is not particularly restricted but preferably is 0.8 to 5 equivalents.
• the amount of the carboxylic acid derivative to be used in this reaction is not particularly restricted. Said derivative may be used in large excess so that it may serve as a solvent as well. Generally, it is used in an amount of about 0.8 to 5 equivalents.
• the reaction schema (C) represents the reaction of a compound [II] with an isocyanate derivative of the formula R 5c NCO [wherein R 5c is as defined above] to give the corresponding compound [V] .
• the amount of the isocyanate derivative to be used in this reaction is not particularly restricted. Said derivative may be used in large excess so that it may serve as a solvent as well. Preferably, it is used in an amount of about 0.8 to 5 equivalents.
• a base for the purpose of promoting the reaction and reducing the byproduct formation or when the starting material is treated with a base prior to the reaction or the reaction mixture after the reaction is treated with a base, favorable results can be obtained. Examples and the amount to be used of such base are the same as those mentioned above in relation to reaction schema (A) .
• the reaction schema (D) represents the reaction of a compound [Ila] with phosgene or an equivalent thereof to give the corresponding intermediate [VI] and the subsequent reaction of [VI] with an amine of the formula R 5d R 5e NH [wherein R 5d and R 5e are as defined above] to give the corresponding compound [VII].
• the phosgene or an equivalent thereof to be used in this reaction includes phosgene, trichloromethyl chloroformate (diphosgene) , bis (trichloromethyl) carbonate (triphosgene) and the like.
• the amount to be used is not particularly restricted, an amount of 0.3 to 5 equivalents is preferred.
• the intermediate [VI] may be used as the starting material in the next reaction either after isolation/purification by per se known means such as concentration, concentration under reduced pressure, pH adjustment, solvent exchange, solvent extraction, distillation, crystallization, recrystallization, chromatography and the like, or in the form of a reaction mixture.
• the amount of the amine of the formula: R 5d R 5e NH to be used in this reaction is not particularly restricted.
• the amine may be used in large excess so that it may serve as a solvent as well. Generally, it is used in an amount of about 0.8 to 5 equivalents .
• the reaction schema (E) represents the reaction of a compound [II] with an alkyl halide of the formula: R 5f Hal [wherein R 5£ is as defined above and Hal represents a halogen atom (e.g. fluorine, chlorine, bromine, iodine)] to give the corresponding compound [VIII].
• R 5f Hal represents a halogen atom (e.g. fluorine, chlorine, bromine, iodine)] to give the corresponding compound [VIII].
• the amount of the alkyl halide of the formula: R 5f Hal to be used in this reaction is not particularly restricted.
• the alkyl halide may be used in large excess so that it may serve as a solvent as well. Generally, it is used in an amount of about 0.8 to 5 equivalents.
• reaction when the reaction is carried out in the presence of a base for the purpose of promoting the reaction and reducing the byproduct formation or when the starting material is treated with a base prior to the reaction or the reaction mixture after the reaction is treated with a base, favorable results can be obtained.
• a base for the purpose of promoting the reaction and reducing the byproduct formation or when the starting material is treated with a base prior to the reaction or the reaction mixture after the reaction is treated with a base.
• examples and the amount to be used of such base are the same as those mentioned above in relation to reaction schema (A) .
• the reaction schema (F) represents the reaction of a compound [IX] with formaldehyde or an equivalent thereof to give the corresponding compound [X] .
• the formaldehyde or an equivalent thereof to be used in this reaction includes formaldehyde and paraformaldehyde, among others.
• the amount to be used is not particularly restricted. This reagent may be used in large excess so that it may serve as a solvent as well. Preferably, it is used in an amount of 0.8 to 15 equivalents .
• an acid for the purpose of promoting the reaction and reducing the byproduct formation or when the starting material is treated with an acid prior to the reaction or the reaction mixture after the reaction is treated with an acid, favorable results can be obtained.
• Such acid catalyst are inorganic protic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid and sulfuric acid; organic protic acids such as formic acid, acetic acid, tartaric acid, malic acid, citric acid, oxalic acid, succinic acid, benzoic acid, trifluoroacetic acid and p-toluenesulfonic acid; and Lewis acids such as aluminum chloride, ferric chloride, zinc chloride, titanium tetrachloride and boron trifluoride.
• the amount of such acid catalyst to be used in the reaction is not particularly restricted unless it adversely affects the reaction.
• the acid catalyst may be used in large excess so that it may serve as a solvent as well.
• the reaction schema (G) represents the oxidation reaction of a compound [XI] with an oxidizing agent to give the corresponding compound [XII].
• the oxidizing agent to be used in this reaction includes, among others, hydrogen peroxide, peracetic acid, perbenzoic acid, m-chloroperbenzoic acid, sodium metaperiodate, ozone, selenium dioxide, chromic acid. bromine, N-bromosuccinimide, iodosylbenzene, t-butyl hypochlorite and the like.
• the amount to be used is not particularly restricted.
• the oxidizing agent may be used in large excess so that it may serve as a solvent as well. Preferably, it is used in an amount of 0.8 to 5 equivalents.
• the reaction schema (H) represents the reaction of a compound [XIII] with a trialkyl orthoformate of the formula: CH(OR 4 ) 3 to give the corresponding compound [XIV].
• the amount of the trialkyl orthoformate to be used in this reaction is not particularly restricted. Said orthoformate may be used in large excess so that it may serve as a solvent as well. Preferably, it is used in an amount of 0.8 to 15 equivalents.
• an acid for the purpose of promoting the reaction and reducing the byproduct formation or when the starting material is treated with an acid prior to the reaction or the reaction mixture after the reaction is treated with an acid, favorable results can be obtained.
• Such acid catalyst are inorganic protic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid and sulfuric acid; organic protic acids such as formic acid, acetic acid, tartaric acid, malic acid, citric acid, oxalic acid, succinic acid, benzoic acid, trifluoroacetic acid, methanesulfonic acid and p-toluenesulfonic acid; and Lewis acids such as aluminum chloride, ferric chloride, zinc chloride, titanium tetrachloride and boron trifluoride.
• the amount of such acid catalyst to be used in the reaction is not particularly restricted unless it adversely affects the reaction.
• the acid catalyst may be used in large excess so that it may serve as a solvent as well.
• reaction schema (I) represents the reaction of a compound [XV] with a vanillin of the formula:
• the amount of the vanillin to be used in this reaction is not particularly restricted. Said vanillin may be used in large excess so that it may serve as a solvent as well. Preferably, it is used in an amount of 0.8 to 15 equivalents.
• an acid for the purpose of promoting the reaction and reducing the byproduct formation or when the starting material is treated with an acid prior to the reaction or the reaction mixture after the reaction is treated with an acid, favorable results can be obtained.
• Such acid catalyst are inorganic protic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid and sulfuric acid; organic protic acids such as formic acid, acetic acid, tartaric acid, malic acid, citric acid, oxalic acid, succinic acid, benzole acid, trifluoroacetic acid and p-toluenesulfonic acid; and Lewis acids such as aluminum chloride, ferric chloride, zinc chloride, titanium tetrachloride and boron trifluoride.
• the amount of such acid catalyst to be used in the reaction is not particularly restricted unless it adversely affects the reaction.
• the acid catalyst may be used in large excess so that it may serve as a solvent as well.
• the reaction schema (J) represents the reaction of a compound [XV] with 2 , 5-dimethox tetrahydrofuran to give the corresponding compound [XVII].
• the amount of 2,5- dimethoxytetrahydrofuran to be used in this reaction is not particularly restricted.
• Said 2,5- dimethoxytetrahydrofuran may be used in large excess so that it may serve as a solvent as well. Preferably, it is used in an amount of 0.8 to 15 equivalents .
• an acid for the purpose of promoting the reaction and reducing the byproduct formation or when the starting material is treated with an acid prior to the reaction or the reaction mixture after the reaction is treated with an acid, favorable results can be obtained.
• Such acid catalyst Usable as such acid catalyst are inorganic protic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, phosphoric acid and sulfuric acid; organic protic acids such as formic acid, acetic acid, tartaric acid, malic acid, citric acid, oxalic acid, succinic acid, benzoic acid, trifluoroacetic acid and p-toluenesulfonic acid; and Lewis acids such as aluminum chloride, ferric chloride, zinc chloride, titanium tetrachloride and boron trifluoride.
• the amount of such acid catalyst to be used in the reaction is not particularly restricted unless it adversely affects the reaction.
• the acid catalyst may be used in large excess so that it may serve as a solvent as well.
• the temperature to be employed in each of the reactions shown in the reaction schemes (B) to (J) is generally within the range of about -50°C to 200°C , preferably about -30°C to 150°C .
• the reaction time is generally within the range of about 0.1 to 96 hours, preferably about 0.1 to 72 hours, more preferably about 0.1 to 24 hours.
• the compounds respectively obtained by the reactions shown in the reaction schemes (B) to (J) can be isolated and purified by such per se known means as mentioned with reference to the reaction schema (A) . They may be used as the starting materials in the next reaction either after such isolation/purification or in the reaction mixture form.
• the compounds [I] or salts thereof are effective in preventing sanitary or horticultural insect pests and animal and plant parasites and can exert potent insecticidal activities when they are applied to harmed living animals or plants. Moreover, the compounds [I] and their salts possess safe and advantageous properties as agents for preventing sanitary, stockbreeding, pet-animal, horticultural or agricultural injurious insects, such as no substantial damage on plants and less toxicity against fishes.
• the compounds [I] or salts thereof can be used as an agricultural chemical, particularly, insecticide in any application form suited for general agricultural chemicals .
• one or two, or more than (preferably one to three) kinds of the compounds [I] or salts thereof are used in the form of preparation such as emulsifiable concentrates, liquid preparation, micro emulsion, flowable concentrates, oil solution, wettable powders, dusts, granules, fine granules, seed coating, smoking pesticides, tablets, microcapsule, sprays, EW, ointments, poisonous bait or the like, according to the purpose of use, by dissolving or dispersing them in suitable liquid carriers or mixing them with or adsorbing them on suitable solid carriers .
• formulations may contain, if necessary, emulsifying agent, suspending agent, spreading agent, penetrating agent, wetting agent, thickening agent, stabilizer, etc., and can be prepared by any conventional method known per se. , e.g. mixing each ingredient .
• liquid carriers include solvents such as water, alcohols (e.g. methanol, ethanol, n-propanol, iso-propanol or ethylene glycol) , ketones (e.g. acetone or methyl ethyl ketone), ethers (e.g. dioxane, tetrahydrofuran, ethylene glycol monomethyl ether, diethylene glycol monomethyl ether or propylene glycol monomethyl ether), aliphatic hydrocarbons (e.g. kerosine, kerosine oil , fuel oil or machine oil) , aromatic hydrocarbons (e.g.
• solvents such as water, alcohols (e.g. methanol, ethanol, n-propanol, iso-propanol or ethylene glycol) , ketones (e.g. acetone or methyl ethyl ketone), ethers (e.g. dioxane, tetrahydrofuran, ethylene glycol
• halogenated hydrocarbons e.g. dichloromethane, chloroform or carbon tetrachloride
• acid amides e.g. N,N-dimethylformamide or N,N- dimethylacetamide
• esters e.g. ethyl acetate, butyl acetate or fatty acid glycerol ester
• Suitable examples of the solid carriers include vegetable powder (e.g. soy-been meal, tobacco meal, wheat flour or wood flour), mineral powders (e.g. clays such as kaolin, bentonite, or acid clay; talcs such as talc powder or pyrophyllite powder; silicas such as diatomaceous earth or mica powder) , aluminas, sulfur powder or activated charcoal. They are used individually or as a suitable mixture of two or more (preferably one to three) of them.
• vegetable powder e.g. soy-been meal, tobacco meal, wheat flour or wood flour
• mineral powders e.g. clays such as kaolin, bentonite, or acid clay
• talcs such as talc powder or pyrophyllite powder
• silicas such as diatomaceous earth or mica powder
• bases for ointments include polyethylene glycol, pectin, polyalcohol esters of higher aliphatic acids (e.g. glycerin mono-stearate) , cellulose derivatives (e.g. methyl cellulose), sodium alginate, bentonite, higher alcohols, polyalcohols (e.g. glycerin), vaseline, white vaseline, liquid paraffin, lard, various vegetable oils, lanolin, dehydrates lanolin, hard oil or resins. These are used individually, or as a suitable mixture of two or more (preferably one to three) of them or together with surface active agents mentioned below.
• nonionic or anionic surface active agents such as soaps
• polyoxyethylene alkyl aryl ethers e.g. Noigen ® and EA 142 ® from Dai-ichi Kogyo Seiyaku K.K. , Japan, and Nonal ® from Toho Chemical, Japan
• alkyl sulfates e.g. Emal 10 ® and Emal 40 ® from Kao K.K. , Japan
• alkyl sulfonates e.g. Neogen ® and Neogen T ® from Dai-ichi Kogyo Seiyaku K.K.
• nonionic or anionic surface active agents such as soaps
• polyoxyethylene alkyl aryl ethers e.g. Noigen ® and EA 142 ® from Dai-ichi Kogyo Seiyaku K.K. , Japan, and Nonal ® from Toho Chemical, Japan
• alkyl sulfates e.g. Emal 10
• Neopellex ® from Kao K.K. a polyethylene glycol ethers (e.g. Nonipol 85 ® , Nonipol 100 ® and Nonipol 160 ® from Sanyo Kasei K.K. , Japan); or polyhydric alcohol estes (e.g., Tween 20 ® and Tween 80 ® from Kao K.K. ) are used, if necessary.
• polyethylene glycol ethers e.g. Nonipol 85 ® , Nonipol 100 ® and Nonipol 160 ® from Sanyo Kasei K.K. , Japan
• polyhydric alcohol estes e.g., Tween 20 ® and Tween 80 ® from Kao K.K.
• the compounds [I] or salts thereof can also be used, as occasion demands, in combination with or as an admixture with other insecticides (for example, pyrethroid insecticides, organophosphorus insecticides, carbamate insecticides, neonicotinoid insecticides or natural insecticides), acaricides , nematicides, herbicides, plant hormones, plant growth regulators , fungicides (for example, copper fungicides , organic chloride fungicides , organic sulfur fungicides or phenolic fungicides), synergistic agents, attractants, repellents, pigments and/or fertilizers .
• insecticides for example, pyrethroid insecticides, organophosphorus insecticides, carbamate insecticides, neonicotinoid insecticides or natural insecticides
• acaricides nematicides
• herbicides for example, pyrethroid insecticides, organophosphorus insecticides, carbamate insecticides,
• the amount of the compound [ I ] or a salt thereof contained in an agrocemical composition (an insecticidal composition) of the present invension is suitably about 0.1 to 80% by weight, preferably about 1 to 20% by weight, relative to the whole composition. Specifically, the amount is suitably about 1 to 80% by weight, preferably about 1 to 20% by weight in the case of emulsifiable concentrates, liquid preparations or wettable powders (e.g. granulated wettable powders); about 0.1 to 50% by weight, preferably about 0.1 to 20% by weight in the case of oil solution or dusts; about 5 to 50% by weight, preferably about 1 to 20% weight in the case of granules .
• the other agricultural active ingredients e.g. insecticide, herbicide, acaricide and/or fungicide
• incorporated into the composition of the present invention may be used in an amount of about 1 to 80% by weight, preferably about 1 to 20% by weight, relative to the whole composition.
• the amount of each of the additives other than the above-described active ingredients usually ranges, which varies depending on the variety and content of the agricultural active ingredient or the form of the composition, is usually about 0.001 to 99.9% by weight, preferably about 1 to 99% by weight, relative to the whole composition. More concretely, the surface active agent may be used in an amount of about 1 to 20% by weight, preferably about 1 to 15% by weight ; the fluidizing agent may be used in an amount of about 1 to 20% by weight; and the carrier may be used in an amount of about 1 to 90% by weight, preferably about 1 to 70% by weight, relative to the whole composition.
• the surface active agent may be used in an amount of about 1 to 20% by weight, preferably about 1 to 10% by weight and water may be used in rate of about 20 to 90% by weight in the case of liquid preparation.
• Emulsifiable concentrates, wettable powders (e.g. granulated wettable powders) or the like can be suitably diluted or extended (for example, to about 100 to 5,000 times) with water or the like, on the occasion of use, and then applied.
• EPN EPN, acephate, isoxathion, isofenphos, isoprocarb, etrimfos, oxydeprofos , quinalphos , cadusafos , chlorethoxyfos , chlorpyrifos , chlorpyrifos-methyl, chlorofenvinphos, salithion, cyanophos, disulfoton, dimethoate, sulprofos , diazinon, thiometon, tetrachlorvinphos , tebupirimfos , trichlorphon, naled, vamidothion, pyraclophos, pyridafenthion , pirimiphos-methyl, fenitrothion, fenthion, phenthoate, fosthiazate, butathiofos, prothiofos, propaphos , profenofos, pho
• tefuranidine AKD-1022, thiomethoxam, bensultap, avermectin, emamectin-benzoate, clofentezine, chlorfluazuron, cyromazine, diafenthiuron, dienochlor, dichlorvos, diflubenzuron, spynosyn, sulfluramid, teflubenzuron, tebufenozide, tebufenpyrad, hydroprene, vaniliprole, pymetrozine, pyridaben, pyriproxyfen , pyrimidifen, fipronil, fenazaquin, fenpyroximate, fluazuron, flucycloxuron , flufenoxuron, buprofezin, hexaflumuron, hexythiazox, milbemycin, metoxadiazone, lufenuron
• Scotinophara lurida Riptortus clavatus . Stephanitis nashi. Laodelphax striatellus . Nilaparvata lugens, Nephotettix cincticeps . Unaspis yanonensis , Aphis glycines . Lipaphis erysimi. Brevicoryne brassicae. Aphis gossypii. Myzys persicae. Aulacorthum solani. Aphis spiraecola. Bemisia tabaci, Trialeurodes vaporariorum. Sogatella furcifera. Empoasca onukii .
• Pseudococcus comstocki Planococcus citri. Icerya purchasi. Plautia stall. Eysarcoris parvus ; Lepidoptera injurious insects such as Spodoptera litura, Plutella xylostella. Pieris rapae crucivora . Chilo suppressalis . Autographa niqrisiqna. Helicoverpa assulta. Pseudaletia separate . Mamestra brassicae . Adoxophyes orana fasciata, Notarcha deroqata. Cnaphalocrocis medinalis . Phthorimaea operculella. Chilo polychrysus .
• Anthrenus verbasci Tribolium castaneum. Lyctus brunneus, Anoplophora malasiac .
• Tomicus piniperda Diptera injurious insects such as Musca domestica, Culex pipiens pallens . Tabanus trigonus . Delia antiqua. Delia platura. Anopheles sinensis, Agromvza oryzae . Hydrellia griseola, Chlorops oryzae . Dacus cucurbitae . Ceratitis capitata. Liriomyza trifolii; Orthoptera injurious insects such as Locusta migratoria, Gryllotalpa africana, Oxya yezoensis.
• the formulations containing the compound [I] or a salt thereof of the present invention are also effective in preventing or combatting arthropod or parasitic animals which parasites inside or outside of a vertebrate (e.g. human, cattle, sheep, goat, pig, fowl, dog, cat, fish, etc.) and in maintaining sanitary, in the field of therapeutics of diseases in livestock and stockbreeding.
• a vertebrate e.g. human, cattle, sheep, goat, pig, fowl, dog, cat, fish, etc.
• parasitic animals include Ixodes spp. , Boophilus spp. (e.g. Boophilus microplus), Amblyomma spp., Hyalomma spp.,
• Rhipicephalus spp. e.g. Rhipicephalus appendiculatus
• Haemaphysalis spp. dermacentor spp.
• Ornithodoros spp. e.g. Ornithodoros moubata
• Dermahyssus gallinae e.g. Sarcoptes spp. (e.g. Sarcoptes scabiei)
• Psoroptes spp. Chorioptes spp.
• Demodex spp. Eutrombicula spp.
• Anopheles spp. Musca spp., Hypoderma spp., Gasterophilus spp., Simulium spp., Triatoma spp., Phthiraptera(e.g. Damalinia spp., Linognathus spp.), Ctenocephalides spp., monomorium pharaonis or Nematodes [e.g. Trichostrongylus such as Nippostrongylus brasiliensis, Trichostrongylus axei or Trichostrongylus colubriformis; Trichinella (e.g. Trichinella spiralis); Haemonchus contortus; Nematodirus (e.g. Nematodirus battus); Ostertagia circumcincta;
• Trichostrongylus such as Nippostrongylus brasiliensis, Trichostrongylus axei or Trichostrongylus colubriformis
• Trichinella e.g. Trichinella spiralis
• the agrochemical composition which comprises a compound [I] or a salt thereof of the present invention can be used as excellent agrachemical composition (insecticidal composition) having excellent insecticidal effects, fairly low toxicity and good safety. It can be used in a similar way to the conventional insecticidal composition and can exert more excellent effects in comparison with the conventional composition.
• occurred injurious insects as mentioned above can be prevented or combatted by applying the agrochemical composition of the present invention to a paddy field, plowland, orchard, non-cropland or house, according to per se known method, and contacting or ingesting to the injurious insects.
• arthropod or parasitic animals which parasites on a vertebrate can be prevented or combatted by administering the agrochemical composition to the inside (in the body) or the outside (on the surface of the body).
• the agrochemical composition of the present invention can be applied to the target insects , by seed treatment, nursery box treatment, planting hole treatment, planting foot treatment, soil treatment, foliar spray, infusion, poisonous bait, smoking, drenching, water application in paddy field.
• the amount of application may broadly vary depending on the season, place and method of application, and so forth.
• the active ingredient (the compound [I] or a salt thereof) is used in amount of about 0.3 g to 3,000 g, preferably about 50 g to 1,000 g per hectare.
• the agrochemical composition of the present invention is in a wettable powder, it can be used by diluting it so as to be about 0.1 - 1000 ppm, preferably about 10 - 500 ppm as the final concentration of the active ingredient.
• This crystal crop was recrystallized from propyl ether-hexane to provide 150 mg (0.24 mmol) of l-(2,6- dichloro- 4-trifluoromethylphenyl ) -3 - ( 4- dimethylaminoacetyl- ⁇ 2 -l , 2 , 4-oxadiazolin-3-yl) -5- ethoxymethyleneamino- 4-trifluoromethylsulfinylpyrazole as colorless crystals, yield: 26% mp.
• Example 16 1- (2, 6 -Dichloro- 4-trifluoromethylphenyl) -3- ⁇ 4-(N,N- diethylcarbamoyl) - ⁇ 2 -l , 2 , 4-oxadiazolin-3-yl ⁇ -5- isopropoxymethyleneamino- 4 - trifluoromethylsulfinylpyrazole
• This reaction mixture was diluted with 20 ml of water and 20 ml of saturated aqueous sodium chloride solution and extracted with 40 ml of ethyl acetate .
• the ethyl acetate layer was washed with 20 ml of saturated aqueous sodium chloride solution (x2) and dried over anhydrous magnesium sulfate.

Landscapes

• Life Sciences & Earth Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Dentistry (AREA)
• Agronomy & Crop Science (AREA)
• Environmental Sciences (AREA)
• Zoology (AREA)
• Wood Science & Technology (AREA)
• Engineering & Computer Science (AREA)
• Plant Pathology (AREA)
• Pest Control & Pesticides (AREA)
• Veterinary Medicine (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Public Health (AREA)
• Animal Behavior & Ethology (AREA)
• Medicinal Chemistry (AREA)
• Tropical Medicine & Parasitology (AREA)
• Pharmacology & Pharmacy (AREA)
• General Chemical & Material Sciences (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Plural Heterocyclic Compounds (AREA)
• Agricultural Chemicals And Associated Chemicals (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Priority Applications (9)

Applications Claiming Priority (6)

Publications (1)

Family

ID=27307845

Family Applications (1)

Country Status (14)

Cited By (14)

Families Citing this family (1)

Citations (2)

Family Cites Families (3)

• 1999
  • 1999-05-31 ES ES99922586T patent/ES2177275T3/es not_active Expired - Lifetime
  • 1999-05-31 BR BR9910912-3A patent/BR9910912A/pt not_active IP Right Cessation
  • 1999-05-31 AU AU39573/99A patent/AU3957399A/en not_active Abandoned
  • 1999-05-31 CN CN998091901A patent/CN1131863C/zh not_active Expired - Fee Related
  • 1999-05-31 WO PCT/JP1999/002876 patent/WO1999062903A1/en not_active Application Discontinuation
  • 1999-05-31 EP EP99922586A patent/EP1084121B1/en not_active Expired - Lifetime
  • 1999-05-31 CA CA002333759A patent/CA2333759A1/en not_active Abandoned
  • 1999-05-31 IL IL13979599A patent/IL139795A0/xx not_active IP Right Cessation
  • 1999-05-31 KR KR1020007013618A patent/KR20010052491A/ko not_active Application Discontinuation
  • 1999-05-31 US US09/701,544 patent/US6288088B1/en not_active Expired - Fee Related
  • 1999-05-31 AR ARP990102567A patent/AR018424A1/es unknown
  • 1999-05-31 DE DE69902387T patent/DE69902387T2/de not_active Expired - Fee Related
  • 1999-05-31 AT AT99922586T patent/ATE221529T1/de not_active IP Right Cessation
  • 1999-06-01 TW TW088109019A patent/TW568908B/zh active

Patent Citations (2)

Also Published As

Similar Documents

Legal Events